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编 号:F089374
分子式:C22H22BrNO
分子量:396.32
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10mM*1mL in DMSO
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1mg
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5mg
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10mg
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50mg
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生物活性:
BCI-215 is a potent and tumor cell-selective dual specificity MAPK phosphatase (DUSP-MKP) inhibitor. BCI-215 has cytotoxicity for tumor cells but not normal cells.

体外研究:
BCI-215 concentration-dependently increases pERK levels in DUSP-overexpressing cells with IC50 value in the micromolar range.BCI-215 (1-20 μM; 6 hours) retains fibroblast growth factor hyperactivating and cellular DUSP6/MKP-3 and DUSP1/MKP-1 inhibitory activity but is nontoxic to zebrafish embryos and an endothelial cell line.BCI-215 inhibits survival and motility of MDA-MB-231 human breast cancer cells but does not affect viability of cultured hepatocytes.BCI-215 is completely devoid of hepatocyte toxicity up to 100 μM.BCI-215 does not generate ROS in hepatocytes or in developing Zebrafish larvae.BCI-215 (22 μM) has antimigratory and proapoptotic activities in breast cancer cells that correlate with induction of ERK phosphorylation.BCI-215 (20 μM; 1 hour) induces mitogenic and stress signaling in cancer cells without generating ROS.
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